HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036246Generated: November 3, 2026
Benzyloxycarbonylglycine → HCID 66654564, compound
https://huagongshe.com/reaction/2036246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyloxycarbonylglycine | HCID 14349 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 66654555 | HCID 66654555 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66654564 | HCID 66654564 | — |
Reaction Steps
A solution of N-carbobenzyloxyglycine (1.07 g, 5.00 mmol, 1.0 eq.) and (±)-[4-fluoro-2-(1,2,3,4-tetrahydro-isoquinolin-1-yl)-phenoxy]-acetic acid ethyl ester hydrochloride (1.93 g, 5.00 mmol, 1.0 eq.) in DMF (30 mL) was treated with 4-(dimethylamino)pyridine (2.44 g, 20.00 mmol, 4.0 eq.) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (1.44 g, 7.50 mmol, 1.5 eq.) and the resulting solution was stirred at r.t. for 18 hours. The reaction mixture was diluted with AcOEt (500 mL). The diluted solution was washed with 1N aq. HCl soln. (3×200 mL), sat. aq. NaHCO3 soln. (3×200 mL), sat. aq. NaCl soln. (1×200 mL), dried over MgSO4, and concentrated in vacuo. The crude product was purified by flash master (column: 100 g, flow: 35 mL/min, heptane to heptane+AcOEt) to yield the title product as a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08575158B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-cf3d6bb6ab224891a0214985c3fa6816 |
|---|
| Source note | uspto-grants-2013_11 |
|---|